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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 339343Generated: October 30, 2026

3-amino-4-hydroxy-N-(1-propylbutyl)benzamide → N-(heptan-4-yl)-2-(methylthio)benzo[d]oxazole-5-carboxamide

https://huagongshe.com/reaction/339343

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-amino-4-hydroxy-N-(1-propylbutyl)benzamideHCID 66773120—
ReactantN-(Heptan-4-yl)-2-(mercapto)benzo[d]oxazole-5-carboxamideHCID 178443996—
SolventEthanolHCID 702—
ProductN-(heptan-4-yl)-2-(methylthio)benzo[d]oxazole-5-carboxamideHCID 5752801155%

Reaction Conditions

Temperature80 °C

Reaction Steps

N-(Heptan-4-yl)-2-(mercapto)benzo[d]oxazole-5-carboxamide: To a solution 3-amino-4-hydroxy-N-(1-propylbutyl)benzamide (example 41a) (250 mg, 1.0 mmol) in EtOH was added KSCSOEt (160 mg, 1.0 mmol). The resulting reaction mixture was heated at 80° C. overnight. The solvent was removed under reduced pressure. And the residue was taken up in water. The resulting mixture was acidified with HOAc to pH ˜5 and then filtered. The residue was washed with water to afford the product as a white solid (160 mg, 55%). MS (M+H, 293.1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08895050B2
Source datasetuspto-grants-2014_11
ORD IDord-91914baf27bd4fb09880c9ae808d1015
Source noteuspto-grants-2014_11